A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615609



Internal ID16056332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133101292..133147666hg38UCSC Ensembl
Innerchr9:135976679..136023053hg19UCSC Ensembl
Innerchr9:134966500..135012874hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3846375
hg1946375
hg1846375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12929n54
Supporting Variantsnssv1176516
SamplesNINDS_66
Known GenesRALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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